The determination of the proportion of uric acid in urine was formerly rather neglected by physicians. There is now, however, a growing tendency in a certain class of diseases to attach considerable importance to its accurate estimation, and, as some little trouble is involved, pharmacists should be prepared to undertake the work. A rough way is to concentrate somewhat, acidulate with hydrochloric acid, and collect and weigh the precipitate thrown down on standing. There are several objections, however, to this method, and many attempts have been made to elaborate a more reliable process. One of the most recent, and which has been pronounced the most practical and successful, has been devised by Professor Haycraft. Although apparently rather detailed and elaborate, the determination is easy and extremely simple. The following solutions must be prepared: 1. Dissolve 5 grammes of nitrate of silver in 100 c.c. of distilled water, and add ammonia until the precipitate first formed redissolves. 2. Dilute strong nitric acid with about two volumes of distilled water; boil, to destroy the lower oxides of nitrogen, and preserve in the dark. 3. Dissolve about 8 grammes of ammonic thiocyanate (sulphocyanide) crystals in a liter of water, and adjust to decinormal argentic nitrate solution, by diluting till one volume is exactly equal to a volume of the latter. Dilute the solution thus prepared with nine volumes of distilled water, and label "Centinormal ammonic-thiocyanate solution." 4. A saturated solution of ferric alum. 5. Strong solution of ammonia (sp. gr. 0.880). The uric acid estimation is conducted as follows: Place 25 per cent. of urine in a beaker with 1 gramme of sodic bicarbonate. Add 2 or 3 c.c. of strong ammonia, and then 1 or 2 c.c. of the ammoniated silver solution. If, on allowing the precipitate caused by the latter reagent to subside, a further precipitate is produced by the addition of more solution, the urine contains an iodide, and silver solution must be added till there is an excess. The gelatinous urate must now be collected, the following special procedure being necessary: Prepare an asbestos filter by filling a 4 oz. glass funnel to about one-third with broken glass, and covering this with a bed of asbestos to about a quarter of an inch deep. This is best managed by shaking the latter in a flask with water until the fibers are thoroughly separated, and then pouring the emulsion so made in separate portions on to the broken glass. On account of the nature of the precipitate and of the filter, it is necessary to use a Sprengel pump, in order to suck the liquid through. The small apparatus sold to students by chemical instrument makers will answer the purpose admirably. Having collected the precipitate of silver urate on the prepared filter, wash it repeatedly with distilled water, until the washings cease to become opalescent with a soluble chloride. Now dissolve the pure urate by washing it through the filter